T2 Plus
K-Number: K233806 · 2024-09-06
Device Summary
Frequently Asked Questions
What is the T2 Plus?
T2 Plus is a medical device that received FDA 510(k) clearance on 2024-09-06. The listed applicant is Osstem Implant Co., Ltd.. The 510(k) number is K233806.
When did T2 Plus receive FDA 510(k) clearance?
T2 Plus received FDA 510(k) clearance on 2024-09-06, under 510(k) number K233806.
Who is the listed applicant for T2 Plus?
The FDA 510(k) record lists Osstem Implant Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for T2 Plus?
The FDA product code for T2 Plus is OAS.
Other records listing Osstem Implant Co., Ltd. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: OAS)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.